The MET-receptor inhibitor capmatinib demonstrated substantial antitumor activity in patients with advanced MET-dysregulated non–small-cell lung cancer.
MET exon 14 skipping mutations and MET gene amplifications occur in 3% to 4% and 1% to 6%, respectively, of patients with non–small-cell lung cancer (NSCLC). Preliminary data demonstrated promising efficacy of the highly selective MET-receptor inhibitor capmatinib in patients with MET-dysregulated NSCLC.
Now, investigators have conducted an industry-funded, multicohort, phase II trial (GEOMETRY mono-1) to evaluate the use of capmatinib (400 mg twice daily) in 364 NSCLC patients with a MET exon 14 skipping mutation or MET amplification.
Results were as follows:
Reviewing Author
DisclosuresConsultant/Advisory BoardGenentech; AstraZeneca; Boehringer-Ingelheim; Bristol-Myers Squibb; Clinical Care Options; Heron; Takeda; Ariad; MedIQ; Targeted Healthcare Communications; Novartis; OncLive; Roche; TRM Oncology
RoyaltiesUpToDate
Grant/Research SupportMedimmune; NIH/National Cancer Institute; Millennium; Genentech; Polaris Pharmaceuticals; Seattle Genetics; Boehringer-Ingelheim Pharmaceuticals; SWOG–Hope Foundation; American Cancer Society; Department of Defense; GlaxoSmithKline Pharmaceuticals; Merck; Eli Lilly; Takeda; Bristol-Myers Squibb
DisclosuresConsultant/Advisory BoardGenentech; AstraZeneca; Boehringer-Ingelheim; Bristol-Myers Squibb; Clinical Care Options; Heron; Takeda; Ariad; MedIQ; Targeted Healthcare Communications; Novartis; OncLive; Roche; TRM Oncology
RoyaltiesUpToDate
Grant/Research SupportMedimmune; NIH/National Cancer Institute; Millennium; Genentech; Polaris Pharmaceuticals; Seattle Genetics; Boehringer-Ingelheim Pharmaceuticals; SWOG–Hope Foundation; American Cancer Society; Department of Defense; GlaxoSmithKline Pharmaceuticals; Merck; Eli Lilly; Takeda; Bristol-Myers Squibb